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Ondansetron

NDC 0121-0882 · PAI Holdings, LLC dba PAI Pharma

Generic nameOndansetron
Dosage formSOLUTION
RouteORAL
Active ingredient(s)ONDANSETRON HYDROCHLORIDE
Strength4 mg/5mL
Pharmacologic classSerotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

0121-0882-51 — 50 mL in 1 BOTTLE, PLASTIC (0121-0882-51)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0054-0064 — Ondansetron Hydrochloride, 0121-4882 — Ondansetron, 0143-9890 — Ondansetron, 0143-9891 — Ondansetron, 0404-9930 — ONDANSETRON, 0409-0009 — ONDANSETRON, 0409-2271 — ONDANSETRON, 0409-4755 — ONDANSETRON, 0409-4759 — ONDANSETRON, 0615-8185 — ondansetron hydrochloride, 0641-6078 — Ondansetron, 0641-6079 — Ondansetron, 0641-6080 — Ondansetron, 0641-6286 — Ondansetron, 0904-6551 — ondansetron hydrochloride, 0904-6552 — ondansetron hydrochloride, 16714-159 — Ondansetron, 16714-160 — Ondansetron, 16714-671 — Ondansetron Hydrochloride, 17856-0672 — Ondansetron Hydrochloride, +154 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.